RNAseqCNV: analysis of large-scale copy number variations from RNA-seq data

Transcriptome sequencing (RNA-seq) is widely used to detect gene rearrangements and quantitate gene expression in acute lymphoblastic leukemia (ALL), but its utility and accuracy in identifying CNVs has not been well described. CNV information inferred from RNA-seq can be highly informative to guide...

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Detalles Bibliográficos
Autores principales: Bařinka, Jan, Hu, Zunsong, Wang, Lu, Wheeler, David A., Rahbarinia, Delaram, McLeod, Clay, Gu, Zhaohui, Mullighan, Charles G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2022
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9177690/
https://www.ncbi.nlm.nih.gov/pubmed/35351983
http://dx.doi.org/10.1038/s41375-022-01547-8

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9177690/
https://www.ncbi.nlm.nih.gov/pubmed/35351983
http://dx.doi.org/10.1038/s41375-022-01547-8

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